Literature DB >> 3315931

Effect of colchicine and phalloidin on the distribution of three plasma membrane antigens in rat hepatocytes: comparison with bile duct ligation.

A M Durand-Schneider1, M Maurice, M Dumont, G Feldmann.   

Abstract

The hepatocyte plasma membrane presents a morphological and functional regionalization into three domains: the sinusoidal; the lateral, and the canalicular. The mechanisms responsible for the biogenesis and maintenance of this regionalization are poorly understood. In this work, we have used colchicine and phalloidin, two drugs known to interfere with the secretory processes in hepatocytes, to study whether they also affect the transport of membrane proteins. The localization of three plasma membrane antigens was studied by light and electron microscopy using monoclonal antibodies identifying either the sinusoidal (A39) or the lateral (B1) or the canalicular (B10) domains in normal hepatocytes. In rats injected with colchicine (0.25 mg per 100 gm), A39 moved from the sinusoidal membrane to the lateral and canalicular ones, whereas B10 was displaced from the canalicular to the sinusoidal and lateral membranes, resulting after 8 hr in an almost equal labeling of the three domains with both antibodies. In rats injected daily for 7 days with phalloidin (50 micrograms per 100 gm), A 39 became mainly localized on the bile canalicular membrane instead of the sinusoidal one; B10 predominated on the canalicular membrane as in controls but in places it labeled the sinusoidal and lateral domains as well. In bile duct-ligated rats studied for comparison for 4, 10 or 21 days, A39 and B10 localizations evolved as after phalloidin, but the changes were more marked. B1 was not affected by any of the treatments. In conclusion, colchicine, phalloidin and bile duct ligation do not seem to hinder the antigens in reaching the plasma membrane, but induce a redistribution of two of them, suggesting a disturbance in the biogenesis and/or control of the plasma membrane regionalization. Such an abnormal distribution could be involved in--or contribute to--the initiation of cholestasis.

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Year:  1987        PMID: 3315931     DOI: 10.1002/hep.1840070611

Source DB:  PubMed          Journal:  Hepatology        ISSN: 0270-9139            Impact factor:   17.425


  11 in total

1.  Bile duct ligation-induced redistribution of canalicular antigen in rat hepatocyte plasma membranes demonstrated by immunogold quantitation.

Authors:  L Landmann; P J Meier; L Bianchi
Journal:  Histochemistry       Date:  1990

Review 2.  Alterations in the establishment and maintenance of epithelial cell polarity as a basis for disease processes.

Authors:  B A Molitoris; W J Nelson
Journal:  J Clin Invest       Date:  1990-01       Impact factor: 14.808

3.  Release of bile canalicular membrane antigen into blood in experimental extrahepatic cholestasis of the rat.

Authors:  Y Kobayashi; H Ohta; T Kawasaki; M Matsumoto; K Tamakoshi; K Kanai
Journal:  Dig Dis Sci       Date:  1994-02       Impact factor: 3.199

Review 4.  Cellular mechanisms of intrahepatic cholestasis.

Authors:  P J Meier-Abt
Journal:  Drugs       Date:  1990       Impact factor: 9.546

5.  Histochemical and immunocytochemical evidence of early, selective bile canaliculi injury after 1,1-dichloroethylene in rats.

Authors:  M T Moslen; H A Dunsford; C Karnasuta; P Chieco; M F Kanz
Journal:  Am J Pathol       Date:  1989-05       Impact factor: 4.307

6.  Redistribution and fate of colchicine-induced alkaline phosphatase in rat hepatocytes: possible formation of autophagosomes whose membrane is derived from excess plasma membrane.

Authors:  N Araki; Y Takashima; T Makita
Journal:  Histochem Cell Biol       Date:  1995-10       Impact factor: 4.304

7.  Kinetic analysis of hepatobiliary transport for conjugated metabolites in the perfused liver of mutant rats (EHBR) with hereditary conjugated hyperbilirubinemia.

Authors:  O Takenaka; T Horie; K Kobayashi; H Suzuki; Y Sugiyama
Journal:  Pharm Res       Date:  1995-11       Impact factor: 4.200

8.  Hepatobiliary transport of glutathione and glutathione conjugate in rats with hereditary hyperbilirubinemia.

Authors:  R P Elferink; R Ottenhoff; W Liefting; J de Haan; P L Jansen
Journal:  J Clin Invest       Date:  1989-08       Impact factor: 14.808

9.  Extrahepatic obstructive cholestasis reverses the bile salt secretory polarity of rat hepatocytes.

Authors:  G Fricker; L Landmann; P J Meier
Journal:  J Clin Invest       Date:  1989-09       Impact factor: 14.808

Review 10.  Cholestasis-induced alterations of the trans- and paracellular pathways in rat hepatocytes.

Authors:  L Landmann
Journal:  Histochem Cell Biol       Date:  1995-01       Impact factor: 4.304

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